Taiwan FDA registration 220e49fc3986acfcfdb47ab8ce100827
GB Manual Blood Cell Counting Device (Non-Sterile)
TW: 普生 手動血球計數裝置 (未滅菌)
Taiwan·Risk Class 1·MD·GENERAL BIOLOGICALS CORP.·Registered Feb 04, 2021 – Feb 04, 2026ExpiredRegistration details
- Analysis ID
- 220e49fc3986acfcfdb47ab8ce100827
- License Form
- Ministry of Health Medical Device Manufacturing No. 008873
Company information
- Manufacturer
- GENERAL BIOLOGICALS CORP.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- GENERAL BIOLOGICALS CORP.
Product details
- Intended Use
- Limited to the first level identification range of the Measures for the Administration of Medical Devices "Manual Blood Cell Counting Device (B.6160)".
- Product Type (Level 1)
- B Hematology and pathology devices
- Product Type (Level 2)
- B6160 Manual blood counting device
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Feb 04, 2021
- Expiry Date
- Feb 04, 2026
About this record
Access comprehensive regulatory information for GB Manual Blood Cell Counting Device (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 220e49fc3986acfcfdb47ab8ce100827 and manufactured by GENERAL BIOLOGICALS CORP.. The authorized representative in Taiwan is GENERAL BIOLOGICALS CORP..
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